Thermodynamically Guided Design of High-Entropy Organic Electrolytes
Source abstract
Abstract
High-entropy electrolytes (HEEs) garner considerable interest for their entropy-stabilized interfacial properties, high ionic conductivity, and exceptional performance across a wide temperature range. Nevertheless, the thermodynamic evolution within these electrolytes during operation remains inadequately characterized, and the broader implications of entropy modulation in designing organic liquid electrolytes remain underexplored. This Letter delineates the thermodynamic equilibria governing organic electrolytes and elucidates how entropy dictates solvation structures and interfacial stability. We further present selection criteria for high-entropy constituents and survey recent breakthroughs in this emerging field. Additionally, we demonstrate the considerable potential of HEEs in enabling operational resilience under extreme temperature conditions. We propose that integrating thermodynamic principles into electrolyte design offers a promising avenue for understanding and tailoring ion-transport phenomena and interfacial behavior in advanced battery systems.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advanced battery technologies research · Electrocatalysts for Energy Conversion
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Guangdong Provincial Key Laboratory on Functional Soft Condensed Matter, School of Materials and Energy
Guangdong University of Technology
Hefei National Research Center for Physical Sciences at the Microscale, Department of Materials Science and Engineering
University of Science and Technology of China
Funding
Fundamental Research Funds for the Central Universities · National Natural Science Foundation of China · Chinese Academy of Sciences · Liaoning Binhai Laboratory
References (44)
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